Variant #0000338145 (NC_000001.10:g.46659598C>G, NC_000001.10(NM_001243766.1):c.880-1G>C (POMGNT1))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46659598C>G
DNA change (hg38) g.46193926C>G
Published as POMGNT1(NM_017739.3):c.880-1G>C
ISCN -
DB-ID POMGNT1_000175 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LURAP1 NM_001013615.2 +/. - c.-9501C>G r.(?) p.(=)
POMGNT1 NM_001243766.1 +/. - c.880-1G>C r.spl? p.?
POMGNT1 NM_017739.3 +/. - c.880-1G>C r.spl? p.?


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